Variant #0000892922 (NC_000016.9:g.30100477G>A, NM_004608.3:c.408C>T (TBX6))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.30100477G>A
DNA change (hg38) -
Published as TBX6(NM_004608.3):c.408C>T (p.R136=)
ISCN -
DB-ID PPP4C_000016
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00079 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP4C NM_002720.1 -?/. - c.*4094G>A r.(=) p.(=)
TBX6 NM_004608.3 -?/. - c.408C>T r.(?) p.(Arg136=)
YPEL3 NM_031477.4 -?/. - c.*3554C>T r.(=) p.(=)


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